Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57077886 0.776 0.240 1 156114947 missense variant C/T snv 9
rs28928900 0.925 0.120 1 156115096 missense variant C/G;T snv 2
rs28933090 0.925 0.160 1 156115172 missense variant T/A;G snv 3
rs59040894 0.925 0.120 1 156115184 missense variant G/A;T snv 2
rs267607560 0.925 0.040 1 156115192 missense variant C/T snv 7.0E-06 2
rs59065411 1.000 0.040 1 156115207 missense variant A/G snv 1
rs267607568 1.000 0.040 1 156115220 missense variant G/A;C;T snv 4.1E-06 1
rs760318158 1.000 0.040 1 156126897 missense variant C/T snv 2.3E-04 6.3E-05 1
rs61661343 0.851 0.040 1 156130687 missense variant T/C snv 4
rs28933093 0.882 0.160 1 156130741 missense variant G/A snv 5
rs267607570 0.925 0.120 1 156130757 missense variant G/A;C snv 4.8E-05 2
rs59026483 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
rs267607571 0.882 0.160 1 156134458 missense variant G/A;T snv 4
rs57045855 0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs28933091 0.882 0.160 1 156134474 missense variant C/A;G snv 4
rs61195471 0.827 0.160 1 156134496 missense variant G/A snv 6
rs28933092 1.000 0.040 1 156134497 missense variant A/G;T snv 2
rs1553265180 1.000 0.040 1 156134500 missense variant T/A;G snv 1
rs267607572 1.000 0.040 1 156134518 missense variant T/G snv 1
rs61295588 0.925 0.160 1 156134809 missense variant T/C snv 2
rs58034145 0.827 0.160 1 156134830 missense variant A/C snv 10
rs60682848 0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 11
rs775964460 1.000 0.040 1 156134883 missense variant C/T snv 8.0E-06 1
rs1165819867 1.000 0.040 1 156134892 missense variant G/A;T snv 1
rs59332535 0.827 0.160 1 156134911 missense variant G/A snv 5